PMA
P160015: AED Plus and Fully Automatic AED Plus
FDA PMA · Automated external defibrillators (non-wearable) · ZOLL Medical Corporation
Key facts
| PMA number | P160015 |
|---|---|
| Trade name | AED Plus and Fully Automatic AED Plus |
| Generic name | Automated external defibrillators (non-wearable) |
| Applicant | ZOLL Medical Corporation |
| Owner/operator | ZOLL Medical Corporation |
| Product code | MKJ |
| Approval date | May 26, 2017 |
| Docket number | 17M-3372 |
| Notice date | Aug 7, 2017 |
| Establishment registration | 1220908 |
| FEI number | 1220908 |
At a glance
- 10–99 Supplements
- Jul 16, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 100–999 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: